Proposal for structure revision of pinofuranoxin A through total syntheses of stereoisomers
Author:
Funder
JSPS
The foundation for Japanese Chemical Research
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s11418-024-01810-5.pdf
Reference39 articles.
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4. Martine VCJ, Yoshida M, Gottlieb OR (1979) Six groups of ω-ethenyl- and ω-ethynyl-α-alkylidene-γ-lactones. Tetrahedron Lett 12:1021–1024
5. Martine VCJ, Yoshida M, Gottlieb OR (1981) ω-Ethyl, ω-ethenyl and ω-ethynyl-α-alkylidene-γ-lactones from Clinostemon mahuba. Phytochemistry 20:459–464
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